{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Arlington",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89089",
      "recalling_firm": "Wright Medical Technology Inc",
      "address_1": "11576 Memphis Arlington Rd",
      "address_2": "N/A",
      "postal_code": "38002-9497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV.  The countries of  Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.",
      "recall_number": "Z-0392-2022",
      "product_description": "Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.",
      "product_quantity": "23 units",
      "reason_for_recall": "The incorrect product is contained in the packaging.",
      "recall_initiation_date": "20211203",
      "center_classification_date": "20211217",
      "report_date": "20211229",
      "code_info": "Lot #1642103"
    }
  ]
}